R&D Engineer II

• Work collaboratively with minimal supervision on routine aspects of research design and develop new product and improvements for current product or detailed instruction for in new projects.
• Contribute to brainstorming sessions and generate new intellectual property working with senior staff and/or attorneys in writing and researching patent claims.
• Complete detailed specifications construction of prototypes and testing of new products or product enhancements ensuring product documentation adheres to Quality System requirements.
• Participate in the design and development of studies and experiments execute product testing and protocols in accordance with project plans.
• Evaluate vendor/contract manufacturer and material choices for designs sharing insights for decision-making.
• Collaborate with customers to determine needs in product design user interface and possible integration of product with other medical systems or products interacting with research physicians to identify potential product and further market opportunities.
• Contribute to the design new products or product enhancements in a cost-effective and timely manner understanding how the product will be manufactured.
• Facilitate user training and oversee the development of supporting materials.
• Contribute to the process of transferring product from development to manufacturing.
• Ensure engineering testing and documentation is in accordance with regulatory requirements for approvals of products by the US and foreign regulatory agencies.
• Complete documentation including design drawings testing reports engineering reports and other technical documents in accordance with quality system requirements.
• Review activities of technicians completing device testing/inspection and prototype construction.

• Bachelors degree in engineering or related discipline and a minimum 1 year of related experience; or equivalent combination of education and work experience.
• Experience in endovascular or neurovascular techniques and devices preferred.
• Statistical Analysis Software (Minitab or similar) and CAD (Solidworks ProE similar).
• Skilled knowledge of machine shop equipment (mill lathe drill press etc.) operation including operation of 3D printing equipment is preferred.
• Developing knowledge of product design from concept to regulatory marketing approval.
• Ability to complete projects individually as well as part of a team exercising judgment within defined procedures and practices to determine appropriate action.
• Ability to apply learned techniques to analysis/investigation to solve challenges using problem-solving tools and methodologies.
• Previous experience working with regulated quality systems such as GMPs ISO 9001 and the MDD.
• Familiar with Design Control procedures and requirements.
• Demonstrated excellent written and verbal communications skills required

The use of external recruiters/staffing agencies requires prior approval from our Human Resources Department. The Human Resources Department at Imperative Care requests that external recruiters/staffing agencies not to contact Imperative Care employees directly in an attempt to present candidates. Complying with this request will be a factor in determining future professional relationships with Imperative Care.

Imperative Care will not accept unsolicited resumes from any source other than candidates themselves for either current or future positions. Submission of unsolicited resumes in advance of an agreement between the Human Resources Department and the external recruiter/staffing agency does not create any implied obligation on the part of Imperative Care.